环金属钌配合物的合成、结构多样性及氧化还原调控
Synthesis, Structural Diversity, and Redox Control of Cyclometalated Monoruthenium Complexes

摘要 环金属钌配合物具有良好的氧化还原和光物理性质，在诸多光电领域如染料敏化太阳能电池、电致变色、电子转移等方面具有重要应用。环金属钌配合物的合成方法主要包括“后期金属化”、“前期金属化”、“转金属化”三种方法。环金属配合物具有丰富的结构多样性。环金属配合物由环金属配体和辅基配体与金属螯合形成。环金属配体包括N∧C、N∧N∧C、N∧C∧N和C∧C∧C-类型多齿配体。辅基配体主要包括吡啶、咪唑、三唑、嘧啶等杂环。碳-金属键的引入大大降低了钌配合物的氧化还原电位。通过改变环金属配体和辅基配体的结构，可以对金属的氧化还原电位进行有效调控。金属钌配合物的氧化还原电位对敏化电池的性能以及电子转移的过程具有重要的影响。
Cyclometalated ruthenium complexes have received increasing attractions recently due to their excellent redox and photophysical properties. One structural feature of these complexes is that there is a ruthenium-carbon (Ru-C) σ bond presented in the molecule. Three common methods, namely, the “late metalation”, “early metalation”, and “transmetalation” methods, for the synthesis of cyclometalated ruthenium complexes are discussed and summarized. General strategies for the design of cyclometalating ligand and cyclometalated ruthenium complexes are introduced. By using different ancillary ligands, such as pyridine, imidazole, triazole, and pyrimidine, a great number of ruthenium complexes can be prepared. The presence of the Ru-C bond significantly decreases the ruthenium oxidation potential. The redox control of these complexes can be realized by using different ancillary ligands and substituents